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About This Item
线性分子式:
(C2H5)3SiC≡CH
CAS号:
分子量:
140.30
Beilstein:
1743814
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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化驗
97%
形狀
liquid
折射率
n20/D 1.433 (lit.)
密度
0.783 g/mL at 25 °C (lit.)
SMILES 字串
CC[Si](CC)(CC)C#C
InChI
1S/C8H16Si/c1-5-9(6-2,7-3)8-4/h1H,6-8H2,2-4H3
InChI 密鑰
FWSPXZXVNVQHIF-UHFFFAOYSA-N
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一般說明
(Triethylsilyl)acetylene, a bulky trialkylsilyl-protected alkyne, undergoes Cadiot-Chodkiewicz cross-coupling reaction with various bromoalkynes to yield synthetically useful unsymmetrical diynes. Rhodium-catalyzed dimerization of (triethylsilyl)acetylene has been reported.
應用
(Triethylsilyl)acetylene may be used in the synthesis of triethylsilylethynyl anthradithiophenes, such as :
- 2,8-dimethyl-5,11-bis(triethylsilylethynyl)ADT (ADT= anthradithiophene)
- 2,8-diethyl-5,11-bis(triethylsilylethynyl)ADT
- 2,8-dipropyl-5,11-bis(triethylsilylethynyl)ADT
訊號詞
Danger
危險聲明
危險分類
Flam. Liq. 2
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
62.6 °F - closed cup
閃點（°C）
17 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
hin-film morphology and transistor performance of alkyl-substituted triethylsilylethynyl anthradithiophenes.
Anthony JE, et al.
Journal of Materials Chemistry, 19(42), 7984-7989 (2009)
Steric tuning of silylacetylenes and chiral phosphine ligands for rhodium-catalyzed asymmetric conjugate alkynylation of enones.
Takahiro Nishimura et al.
Journal of the American Chemical Society, 130(5), 1576-1577 (2008-01-17)
Joseph P Marino et al.
The Journal of organic chemistry, 67(19), 6841-6844 (2002-09-14)
Bulky trialkylsilyl-protected alkynes such as triethylsilyl (TES), tert-butyldimethylsilyl (TBS), and triisopropylsilyl (TIPS) acetylenes underwent the Cadiot-Chodkiewicz cross-coupling reaction with different bromoalkynes to form a variety of synthetically useful unsymmetrical diynes in good yields. The diyne alcohol 10 was transformed regio-
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